Canonical Allele Identifier: CA508090006
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1279507599
gnomAD v4: 19-49060997-C-A
MyVariant Identifiers: chr19:g.49564254C>A (hg19) chr19:g.49060997C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060997C>A , CM000681.2:g.49060997C>A GRCh38
NC_000019.9:g.49564254C>A , CM000681.1:g.49564254C>A GRCh37
NC_000019.8:g.54256066C>A NCBI36
NG_016289.1:g.7871G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+758G>T ENSP00000470689.1:n.243+758G>T
XR_001753693.1:n.879+167G>T
XR_001753694.1:n.879+167G>T
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